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LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.
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2004 (English)In: Nat Med, ISSN 1078-8956, Vol. 10, no 7, 696-703 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 10, no 7, 696-703 p.
Keyword [en]
Animals, Cytoskeletal Proteins/*metabolism, Dystroglycans, Gene Therapy, Glycosylation, Glycosyltransferases/*deficiency, Humans, Laminin/metabolism, Membrane Glycoproteins/*metabolism, Mice, Muscular Dystrophies/*congenital/genetics/therapy, N-Acetylglucosaminyltransferases/genetics/*physiology, Neoplasm Proteins/genetics/*physiology, Research Support; Non-U.S. Gov't, Research Support; U.S. Gov't; P.H.S.
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URN: urn:nbn:se:uu:diva-71952PubMedID: 15184894OAI: oai:DiVA.org:uu-71952DiVA: diva2:99863
Available from: 2005-05-16 Created: 2005-05-16 Last updated: 2011-01-12

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